International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and Classification of Adenosine Receptors-An Update

被引:1083
作者
Fredholm, Bertil B. [1 ]
IJzerman, Adriaan P. [2 ]
Jacobson, Kenneth A. [3 ]
Linden, Joel [4 ]
Mueller, Christa E. [5 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[2] Leiden Amsterdam Ctr Drug Res, Div Med Chem, Leiden, Netherlands
[3] NIDDK, Mol Recognit Sect, Bioorgan Chem Lab, NIH, Bethesda, MD USA
[4] La Jolla Inst Allergy & Immunol, Div Inflammat Biol, La Jolla, CA USA
[5] Univ Bonn, Inst Pharmaceut, PharmaCtr Bonn, D-5300 Bonn, Germany
基金
美国国家卫生研究院;
关键词
PROTEIN-COUPLED RECEPTOR; DOPAMINE D-1 RECEPTORS; HIGHER-ORDER OLIGOMERS; A(1) RECEPTOR; A(2A) RECEPTOR; ALLOSTERIC MODULATION; BIOLOGICAL EVALUATION; MICE LACKING; A(3) RECEPTOR; XANTHINE DERIVATIVES;
D O I
10.1124/pr.110.003285
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the 10 years since our previous International Union of Basic and Clinical Pharmacology report on the nomenclature and classification of adenosine receptors, no developments have led to major changes in the recommendations. However, there have been so many other developments that an update is needed. The fact that the structure of one of the adenosine receptors has recently been solved has already led to new ways of in silico screening of ligands. The evidence that adenosine receptors can form homo- and heteromultimers has accumulated, but the functional significance of such complexes remains unclear. The availability of mice with genetic modification of all the adenosine receptors has led to a clarification of the functional roles of adenosine, and to excellent means to study the specificity of drugs. There are also interesting associations between disease and structural variants in one or more of the adenosine receptors. Several new selective agonists and antagonists have become available. They provide improved possibilities for receptor classification. There are also developments hinting at the usefulness of allosteric modulators. Many drugs targeting adenosine receptors are in clinical trials, but the established therapeutic use is still very limited.
引用
收藏
页码:1 / 34
页数:34
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